Resumen de: US20260325742A1
0000 A wearable infusion pump assembly. The wearable infusion pump assembly includes a reservoir for receiving an infusible fluid and a fluid delivery system configured to deliver the infusible fluid from the reservoir to an external infusion set. The fluid delivery system includes a controller, a pump assembly for extracting a quantity of infusible fluid from the reservoir and providing the quantity of infusible fluid to the external infusion set, the pump assembly comprising a pump plunger, the pump plunger having distance of travel, the distance of travel having a starting position and an ending position, at least one optical sensor assembly for sensing the starting position and ending position of the pump plunger distance of travel and sending sensor output to the controller, and a first valve assembly configured to selectively isolate the pump assembly from the reservoir, wherein the controller receives the sensor output and determines the total displacement of the pump plunger.
Resumen de: US20260325102A1
Exemplary embodiments provide systems and methods for portable medical ultrasound imaging. Preferred embodiments utilize a tablet touchscreen display operative to control imaging and display operations without the need for using traditional keyboards or controls. Certain embodiments provide a multi-chip module for an ultrasound engine of a portable medical ultrasound imaging system, in which a transmit/receive chip, an amplifier chip and a beamformer chip are assembled in a vertically stacked configuration. Exemplary embodiments also provide an ultrasound engine circuit board including one or more multi-chip modules, and a portable medical ultrasound imaging system including an ultrasound engine circuit board with one or more multi-chip modules. Exemplary embodiments also provide methods for fabricating and assembling multi-chip modules as taught herein.
Resumen de: US20260325080A1
A computing device for use in a system for mapping brain activity of a subject includes a processor. The processor is programmed to select a plurality of measurements of brain activity that is representative of at least one parameter of a brain of the subject during a resting state. Moreover, the processor is programmed to compare at least one data point from each of the measurements with a corresponding data point from a previously acquired data set from at least one other subject. The processor is also programmed to produce at least one map for each of the measurements based on the comparison of the resting state data point and the corresponding previously acquired data point. The processor may also be programmed to categorize the brain activity in a plurality of networks in the brain based on the map.
Resumen de: AU2026242142A1
A tensioner tool for assessing joint laxity is disclosed. The tensioner tool comprises a pair of pivotally coupled arms, each arm comprising a proximal handle portion, a distal portion, and an insertion tip selectively coupled to the distal portion. The pair of arms pivot between a compressed configuration for insertion within the joint and an expanded configuration for distraction of the joint by applying a force to the handles, thus spreading the insertion tips. The tensioner tool also comprises a force sensor configured to measure the force applied to the handle portion and a positional sensor configured to measure a separation distance between the pair of arms. The tensioner tool also comprises a processor configured to calculate a distraction force at the insertion tips based on the measured force and to calculate a tip distance between the insertion tips based on the measured separation distance. ep e p
Resumen de: US20260325382A1
Modules for housing electronic and electromechanical medical equipment including a system to measure and record administration of one or more IV medications or fluids for IV administration.
Resumen de: US20260325780A1
A patient interface including a seal-forming structure with a textile membrane that has at least one hole such that the flow of air at a therapeutic pressure is delivered to at least an entrance to the patient's nares and/or an entrance to the patient's mouth. The seal-forming structure is constructed and arranged to maintain the therapeutic pressure in a cavity of a plenum chamber throughout the patient's respiratory cycle, in use. The textile membrane includes a first portion that is held in a relaxed state and a second portion that is held in a taut state. The taut state of the second portion is configured to allow the seal-forming structure to include a three-dimensional shape that has multiple curvatures.
Resumen de: US2020347507A1
In one embodiment, a method for manufacturing an aperture plate includes depositing a releasable seed layer above a substrate, applying a first patterned photolithography mask above the releasable seed layer, the first patterned photolithography mask having a negative pattern to a desired aperture pattern, electroplating a first material above the exposed portions of the releasable seed layer and defined by the first mask, applying a second photolithography mask above the first material, the second photolithography mask having a negative pattern to a first cavity, electroplating a second material above the exposed portions of the first material and defined by the second mask, removing both masks, and etching the releasable seed layer to release the first material and the second material. The first and second material form an aperture plate for use in aerosolizing a liquid. Other aperture plates and methods of producing aperture plates are described according to other embodiments.
Resumen de: US20260326382A1
0000 A method for 3D printing a patient-specific bone implant having variable density, in various aspects, comprises: (1) providing a thermoplastic polymer composition comprising: (A) between about 20% and about 50% bioactive agent by weight; (B) between about 0.5% and about 10% chemical foaming agent by weight; and (C) balance structural polymer by weight; (2) receiving, by computing hardware, a scan of a bone, the scan comprising at least a 3D image of the bone and radiodensity data for the bone; and (3) causing, by the computing hardware, a 3D printer to form the patient-specific bone implant from the 3D image using the thermoplastic polymer by modifying a 3D printing temperature of the 3D printer during printing of the patient-specific bone implant such that each portion of the patient-specific bone implant is produced at a temperature that corresponds to a desired density defined by the radiodensity data for the bone.
Resumen de: AU2026242121A1
Recommendations based on continuous glucose monitoring (CGM) are described. Given the number of people that wear CGM systems and because CGM systems produce measurements continuously, a platform that provides a CGM system may have an enormous amount of data. This amount of data is practically, if not actually, impossible for humans to process. In implementations, a CGM platform includes a data analytics platform that obtains glucose measurements provided by a CGM system and also obtains additional data associated with a user. The data analytics platform processes these measurements and the additional data to predict a health indicator by using models. This prediction serves as a basis for generating a recommendation, such as a message recommending the user take action or adopt a behavior to mitigate a predicted negative health condition. ep e p
Resumen de: US20260325773A1
The present disclosure provides for a control system for a flow therapy apparatus. The control system can control delivery of a fraction of delivered oxygen (FdO2) to a patient. The control system can maintain the FdO2 at a target level during a therapy session. The control system can automatically control an oxygen inlet valve in order to control the flow of oxygen to the patient.
Resumen de: US20260331252A1
A computer-implemented method is disclosed. The method includes determining whether one or more messages have been received while a user performs a treatment plan. The one or more messages may pertain to at least one of a user and a usage of the electromechanical machine by the user. The electromechanical machine may be configured to be manipulated by the user while the user is performing a treatment plan. The method also includes, responsive to determining that the one or more messages have not been received, determining, using one or more machine learning models, one or more preventative actions to perform. The method also includes causing the one or more preventative actions to be performed.
Resumen de: US20260325019A1
Systems and methods for wireless communication of analyte information are disclosed. Example embodiments include an analyte sensor system. The analyte sensor system may include an analyte sensor to gather information related to a level of an analyte in a host. The analyte sensor system may include circuitry to transmit and receive wireless signals using a first antenna. The analyte sensor may be coupled to the circuitry before the analyte sensor system is transitioned into an operational state. The analyte sensor system may include a second antenna to receive an input signal from a source external to the analyte sensor system and to transmit a modified signal. The circuitry may use the first antenna to receive the modified signal The analyte sensor system may transition into the operational state in response to the modified signal received using the first antenna.
Resumen de: US20260325073A1
A device for monitoring a patient includes a substrate, an adhesive layer coupled to a first side of the substrate, and a circuit board coupled to a second side of the substrate. The adhesive layer is configured to adhere to a patient. The device includes a first plurality of input interfaces coupled to the circuit board. The first plurality of input interfaces configured to identify a particular injury location. The device includes a second plurality of input interfaces coupled to the circuit board. The second plurality of input interfaces configured to identify a patient injury type. The device also includes a wireless transmitter coupled to the circuit board. The wireless transmitter is configured to transmit medical information associated with the patient to a mobile device. The medical information includes data indicating a setting of each of the first plurality of input interfaces and the second plurality of input interfaces
Resumen de: US20260325268A1
0000 A method and device for processing oral scanning data, and an apparatus are provided. The method includes: performing a scanning task on a plurality of scan regions in an oral cavity in a preset scanning sequence; obtaining target scanning data of the current scan region when a scanning completion event of the current scan region is monitored; performing a data processing task on the target scanning data when no data processing task is being performed; and performing the scanning task on the next scan region according to the scanning sequence, and determining the next scan region as a new current scan region.
Resumen de: US20260325244A1
A method for using a control center at a remote site to control operation of a robotic medical device system at a local site includes transmitting a control signal from the control center to the robotic medical device system, determining a delay in transmission of the control signal, comparing the delay to a threshold delay value and operating the robotic medical device system based on the comparison of the delay to the threshold delay value.
Resumen de: US20260324973A1
0000 Systems, devices, and methods for remote monitoring and managing of patients with chronic pain are discussed. A remote monitoring system comprises a cloud-computing device and a remote device. The cloud-computing device receives patient data including physiological or functional information sensed by sensors, and provides on-demand cloud-based services including establishing a correspondence between one or more physiological or functional states and one or more pain levels, detecting patient physiological or functional state, predicting a pain level, detecting a patient behavior, generating a recommendation for adjusting sensor operations based on the patient behavior, and storing patient data and other information in a cloud storage. The remote device can access the cloud storage and the cloud-based services, provide the stored information to an authorized user or the patient, control an implantable device to initiate or adjust a neuromodulation therapy, or adjust sensor operations.
Resumen de: US20260325872A1
0000 Embodiments of the present disclosure provide methods for training an artificial radiotherapy environment model. The method can include: providing an artificial radiotherapy environment model including: a transition function model configured to predict a next state based on a given state and a given radiation dose for a patient, a radiotherapy outcome estimator model configured to predict a treatment outcome for the next state, the radiotherapy outcome estimator model including at least two artificial neural networks and a logistic function, wherein respective outputs of the at least two artificial neural networks are fed into the logistic function, and a reward function configured to assign a reward for the next state based on the treatment outcome for the next state; and training the artificial radiotherapy environment model with a labeled dataset including a plurality of patient records.
Resumen de: US20260331251A1
Aspects of systems and methods for authenticating illuminating medical infusion lines are disclosed. An electronic illuminator for illuminating medical infusion lines includes a fiber detection assembly configured with a three-dimensional magnetic flux density and a microcontroller. A side scattering fiber optic cable includes a fiber funnel cap with a metallic plate at a proximal end and a protective end cap at a distal end. The fiber detection assembly detects a magnetic flux key when the fiber funnel cap is connected to the electronic illuminator. An electronic illuminator is provisioned with a fiber detection assembly configured with a three-dimensional magnetic flux density. A side scattering fiber optic cable with a fiber funnel cap configured with a metallic plate is connected to the electronic illuminator. A change in voltage is detected as the fiber funnel cap is connected, wherein a final voltage results in a magnetic flux key that is authenticated by the MCU against stored parameters.
Resumen de: US20260325257A1
0000 A method for manufacturing a dental prosthesis part that can be connected to a tooth stump, in particular a fixed dental prosthesis part includes manufacturing an adapter for a machine tool and a blank for the dental prosthesis part.
Resumen de: US20260331289A1
An artificially intelligent system and method for prognostic evaluation of autoimmune disorders. Certain objects and advantages of the present disclosure include methods and systems configured to aggregate and analyze clinical conversational data, patient biometric data, medical records data, blood biomarker test data, and patient biometric data to tune metrics that are increasingly specific to a patient in the creation of a dynamic patient phenotype to enhance clinical understanding of one or more factors that are specific to the patient's health status. One or more Al framework and engine may facilitate effective integration of communication-related insights into diagnostic and prognostic digital health resources. Exemplary systems, methods, and apparatuses according to the principles herein may comprise machine learning and deep learning techniques for the development of one or more quantitative metrics derived from clinical conversational data.
Resumen de: GB2645382A
A patient is provided with a wristband having a unique machine-readable patient code and medical cabinet 2. Cabinet 2 has first compartment 4 for securely containing the Patient's Own Drugs (PODs) and second compartment 6 for securely containing further medicines. Authorised persons register the patient on a computer and register PODs by entering details of each POD into the computer. Authorised persons set reminder times in the computer for administration of PODs and place PODs into first compartment 4. Optionally, further medicines are placed into second compartment 6. The computer provides a reminder to the patient at each reminder time. Upon receipt of the reminder, the patient scans the wristband using a code reader. The reading of the unique patient code initiates unlocking of the door to first compartment 4, but not second compartment 6, thereby giving the patient access to a POD. Optionally, the ability of a patient to comply with self-administration of a drug treatment regime is assessed by logging the number of times a first locker is unlocked by scanning the patient's wristband and comparing the number with the number of reminders.
Resumen de: EP4826736A1
0001 The present invention relates to a computer-implemented method for predicting a patient's (P) fistula failure encompassing an inputting of a plurality of parameter values, into a computer system (1), wherein some of these values have been measured during one or more dialysis treatment sessions while treating the patient (P) using a hemodialysis treatment apparatus (100) and/or wherein some of these values are or have been calculated based on or derived from values having been measured during one or more dialysis treatment sessions while treating the patient (P) using a hemodialysis treatment apparatus (100). The computer-implemented method further encompasses a predicting of the probability of an event predefined as a fistula failure within a predetermined time period or within a predetermined number of treatment sessions. Moreover, it encompasses an outputting of the predicted probability.
Resumen de: TR2026016910A2
Buluş, gebelik döneminde idrar stripleri ile glikoz takibinin ev ortamında güvenilir bir şekilde yapılabilmesi amacıyla, standart idrar striplerinin optik olarak okunmasını, okunan verinin gebelik haftasına göre dinamik eşik değerleri, önceki ölçüm trendleri, ölçüm zamanı, strip geçerlilik kontrolü ve referans alan doğrulaması ile birlikte değerlendiren ve yalnızca doğrulanmış kritik risk durumunda kapalı devre bildirim gönderen bir akıllı takip sistemi ile bu sistemin çalışma yöntemini kapsamaktadır.
Resumen de: EP4825318A1
0001 The present disclosure provides a method and a computing device for setting a treatment order based on an emergency patient's condition. According to an embodiment of the present disclosure, a method for setting a treatment order based on an emergency patient's condition, performed by a computing device including at least one processor, comprises, when reception data of a new examinee is acquired, acquiring physiological data of the examinee via a sensing unit, analyzing the physiological data using a pre-trained neural network model to identify the new examinee's condition, and setting a treatment order for the new examinee based on a time at which the reception data of the new examinee is acquired and the new examinee's condition. The setting of the treatment order comprises setting the treatment order for the new examinee by adjusting, based on the examinee's condition, the treatment orders of the other previously registered examinees who are waiting for treatment.
Nº publicación: EP4826734A2 21/10/2026
Solicitante:
SMITH & NEPHEW [GB]
T.J. Smith & Nephew, Limited
Resumen de: EP4826734A2
0001 Embodiments of delivering reduced pressure wound therapy are disclosed. In some embodiments, a system includes a reduced pressure wound therapy device and a remote computer. The device can be configured to apply reduced pressure to a wound of a patient according to a default reduced pressure therapy prescription. The device can be configured to monitor usage data and transmit the usage data to the remove computer for determining compliance with a reduced therapy prescription. In some cases, non-compliance can be determined due to change of the prescription from the default prescription to a prescription more suitable for treating the wound. A non-compliance notification can be transmitted to the device. The device settings can be updated to the current prescription.